-
Something wrong with this record ?
Variants within the ghrelin gene - association with HDL-cholesterol, but not with body mass index
Jaroslav A. Hubáček, Romana Bohuslavová, Zdeňka Škodová, Adámková V.
Language English Country Czech Republic
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
ProQuest Central
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
- MeSH
- Financing, Organized utilization MeSH
- Ghrelin genetics MeSH
- Cholesterol, HDL genetics blood MeSH
- Body Mass Index MeSH
- Evidence-Based Medicine trends MeSH
- Polymerase Chain Reaction methods utilization MeSH
- Polymorphism, Genetic genetics MeSH
- Waist-Hip Ratio statistics & numerical data MeSH
- Geographicals
- Czech Republic MeSH
Ghrelin is a hormone which influences eating habits, the amount of food ingested and the body's energy balance. We examined whether genetic variants in the ghrelin gene are associated with BMI, WHR and plasma lipid levels. We have evaluated the influence of ghrelin polymorphisms (Arg51>Gln, Leu72>Met and Gln90>Leu) on BMI, WHR, and plasma lipid levels in 1,191 males and 1,368 females representatively selected from the Czech population. Anthropometrical and biochemical parameters were analysed in two different years. In the entire population, we have detected 4.8% of carriers of the Gln51 allele, 14.2% carriers of the Met72 allele, and 10.9% of the Leu90 allele. Frequencies did not differ between males and females and alleles were not in linkage disequilibrium. BMI or WHR were not influenced by variants in the ghrelin gene. The ghrelin variant Leu72>Met was associated with elevated levels of plasma HDL-cholesterol. Compared to Leu/ Leu homozygotes, the Met carriers had lower HDL-cholesterol concentrations in males (1.18 +/- 0.29 mmol/l vs. 1.24 +/- 0.35 mmol/l, P = 0.01) as well as in females (1.45 +/- 0.35 mmol/l vs. 1.51 +/- 0.38 mmol/l, P = 0.01). The other lipid parameters (total cholesterol and triglycerides) were not associated with this variant. There were no associations between other ghrelin variants (Arg51>Gln and Gln90>Leu) and analysed biochemical parameters. We conclude that in the Caucasian population, variations in the ghrelin gene could play a role in genetic determination of plasma levels of HDL-cholesterol, but they have no effect on BMI or WHR.
Lit.: 17
- 000
- 03474naa 2200421 a 4500
- 001
- bmc07506980
- 003
- CZ-PrNML
- 005
- 20111210122753.0
- 008
- 080724s2007 xr e eng||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Hubáček, Jaroslav, $d 1966- $7 nlk20050169367
- 245 10
- $a Variants within the ghrelin gene - association with HDL-cholesterol, but not with body mass index / $c Jaroslav A. Hubáček, Romana Bohuslavová, Zdeňka Škodová, Adámková V.
- 314 __
- $a Institute for Clinical and Experimental Medicine, Prague
- 504 __
- $a Lit.: 17
- 520 9_
- $a Ghrelin is a hormone which influences eating habits, the amount of food ingested and the body's energy balance. We examined whether genetic variants in the ghrelin gene are associated with BMI, WHR and plasma lipid levels. We have evaluated the influence of ghrelin polymorphisms (Arg51>Gln, Leu72>Met and Gln90>Leu) on BMI, WHR, and plasma lipid levels in 1,191 males and 1,368 females representatively selected from the Czech population. Anthropometrical and biochemical parameters were analysed in two different years. In the entire population, we have detected 4.8% of carriers of the Gln51 allele, 14.2% carriers of the Met72 allele, and 10.9% of the Leu90 allele. Frequencies did not differ between males and females and alleles were not in linkage disequilibrium. BMI or WHR were not influenced by variants in the ghrelin gene. The ghrelin variant Leu72>Met was associated with elevated levels of plasma HDL-cholesterol. Compared to Leu/ Leu homozygotes, the Met carriers had lower HDL-cholesterol concentrations in males (1.18 +/- 0.29 mmol/l vs. 1.24 +/- 0.35 mmol/l, P = 0.01) as well as in females (1.45 +/- 0.35 mmol/l vs. 1.51 +/- 0.38 mmol/l, P = 0.01). The other lipid parameters (total cholesterol and triglycerides) were not associated with this variant. There were no associations between other ghrelin variants (Arg51>Gln and Gln90>Leu) and analysed biochemical parameters. We conclude that in the Caucasian population, variations in the ghrelin gene could play a role in genetic determination of plasma levels of HDL-cholesterol, but they have no effect on BMI or WHR.
- 650 _2
- $a ghrelin $x genetika $7 D054439
- 650 _2
- $a polymorfismus genetický $x genetika $7 D011110
- 650 _2
- $a poměr pasu a boků $x statistika a číselné údaje $7 D049629
- 650 _2
- $a index tělesné hmotnosti $7 D015992
- 650 _2
- $a HDL-cholesterol $x genetika $x krev $7 D008076
- 650 _2
- $a medicína založená na důkazech $x trendy $7 D019317
- 650 _2
- $a polymerázová řetězová reakce $x metody $x využití $7 D016133
- 650 _2
- $a financování organizované $x využití $7 D005381
- 651 _2
- $a Česká republika $7 D018153
- 700 1_
- $a Bohuslavová, Romana, $d 1966- $7 xx0074151
- 700 1_
- $a Škodová, Zdenka $7 xx0153069
- 700 1_
- $a Adámková, Věra, $d 1954- $7 jx20050329003
- 773 0_
- $w MED00011004 $t Folia biologica $g Roč. 53, č. 6 (2007), s. 202-206 $x 0015-5500
- 856 41
- $u http://fb.cuni.cz/data/files/folia_biologica/volume_53_2007_6/fb2007a0031.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 970 $c 89 $y 1
- 990 __
- $a 20080724155410 $b ABA008
- 991 __
- $a 20080725122742 $b ABA008
- 999 __
- $a ok $b bmc $g 622588 $s 475021
- BAS __
- $a 3
- BMC __
- $a 2007 $b 53 $c 6 $d 202-206 $i 0015-5500 $m Folia biologica (Praha) $x MED00011004
- LZP __
- $a 2008-11/mkal